TY - JOUR
T1 - A facile method to prepare hydrophobic nanoparticle dispersions for controlled release
AU - Liu, Yu Yang
AU - Su, Xia
AU - Tang, Min Feng
AU - Kong, Jie
PY - 2007/2/21
Y1 - 2007/2/21
N2 - Using ethyl acrylate and methyl methacrylate as hydrophobic monomers, a series of hydrophobic nanoparticle dispersions were prepared by one-step polymerization (i.e., soap-free batch emulsion polymerization). To obtain stable aqueous nanoparticle dispersions, a small amount of ionic comonomer, sodium 4-ω-acryloyloxyβ-hydroalkyl sulfonate (Cops-1) was used. The nanoparticles were characterized by TEM, Zetasizer and DSC. It was found that number average diameter (D̄n) values range from 144 to 202 nm at 25°C, and the diameter distribution [D̄v/D̄ n) from 1.11 to 1.14. These results indicate that the nanoparticles show a narrow distribution of sizes. Zeta potentials of the obtained nanoparticles are in range of -38.8 to -29.7 mV at 25°C. This suggests that they can be well dispersed in water. Using salicylic acid (SA) as model drug molecules, a novel swelling method was developed for loading SA into the nanoparticles in an aqueous dispersion state, and both related loading processes and controlled release behavior were investigated. It was found that the nanoparticles can sustain SA release, and compared to different types of nanoparticles, PMMA nanoparticles can retard SA release more effectively.
AB - Using ethyl acrylate and methyl methacrylate as hydrophobic monomers, a series of hydrophobic nanoparticle dispersions were prepared by one-step polymerization (i.e., soap-free batch emulsion polymerization). To obtain stable aqueous nanoparticle dispersions, a small amount of ionic comonomer, sodium 4-ω-acryloyloxyβ-hydroalkyl sulfonate (Cops-1) was used. The nanoparticles were characterized by TEM, Zetasizer and DSC. It was found that number average diameter (D̄n) values range from 144 to 202 nm at 25°C, and the diameter distribution [D̄v/D̄ n) from 1.11 to 1.14. These results indicate that the nanoparticles show a narrow distribution of sizes. Zeta potentials of the obtained nanoparticles are in range of -38.8 to -29.7 mV at 25°C. This suggests that they can be well dispersed in water. Using salicylic acid (SA) as model drug molecules, a novel swelling method was developed for loading SA into the nanoparticles in an aqueous dispersion state, and both related loading processes and controlled release behavior were investigated. It was found that the nanoparticles can sustain SA release, and compared to different types of nanoparticles, PMMA nanoparticles can retard SA release more effectively.
KW - Drug release
KW - Hydrophobic nanoparticle dispersion
KW - Soap-free emulsion polymerization
UR - http://www.scopus.com/inward/record.url?scp=34547838634&partnerID=8YFLogxK
U2 - 10.1002/macp.200600400
DO - 10.1002/macp.200600400
M3 - 文章
AN - SCOPUS:34547838634
SN - 1022-1352
VL - 208
SP - 415
EP - 422
JO - Macromolecular Chemistry and Physics
JF - Macromolecular Chemistry and Physics
IS - 4
ER -